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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Respiratory Virus Panel Nucleic Acid Assay System
510(k) Number K191729
Device Name Cobas Influenza A/B Nucleic Acid Test for Use on the Cobas Liat System
Applicant
Roche Molecular Systems, Inc.
4300 Hacienda Dr.
Pleasanton,  CA  94588 -2722
Applicant Contact Kaitlyn Hameister
Correspondent
Roche Molecular Systems, Inc.
4300 Hacienda Dr.
Pleasanton,  CA  94588 -2722
Correspondent Contact Kaitlyn Hameister
Regulation Number866.3980
Classification Product Code
OCC  
Subsequent Product Code
OOI  
Date Received06/27/2019
Decision Date 07/24/2019
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Summary Summary
FDA Review Decision Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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